US4897328A - Electrophotographic lithographic printing plate precursor - Google Patents
Electrophotographic lithographic printing plate precursor Download PDFInfo
- Publication number
- US4897328A US4897328A US07/188,824 US18882488A US4897328A US 4897328 A US4897328 A US 4897328A US 18882488 A US18882488 A US 18882488A US 4897328 A US4897328 A US 4897328A
- Authority
- US
- United States
- Prior art keywords
- group
- printing plate
- plate precursor
- substituted
- lithographic printing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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- 239000002243 precursor Substances 0.000 title claims abstract description 62
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- 239000002344 surface layer Substances 0.000 claims abstract description 53
- 125000000524 functional group Chemical group 0.000 claims abstract description 33
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- 238000000586 desensitisation Methods 0.000 claims abstract description 24
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- 125000000217 alkyl group Chemical group 0.000 claims description 13
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- 125000003118 aryl group Chemical group 0.000 claims description 10
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- 125000004434 sulfur atom Chemical group 0.000 claims description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 6
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- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
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- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
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- 238000007598 dipping method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000008376 fluorenones Chemical class 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
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- 235000011187 glycerol Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229940083761 high-ceiling diuretics pyrazolone derivative Drugs 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 150000007978 oxazole derivatives Chemical class 0.000 description 1
- RPDJEKMSFIRVII-UHFFFAOYSA-N oxomethylidenehydrazine Chemical compound NN=C=O RPDJEKMSFIRVII-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
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- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
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- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- RCYFOPUXRMOLQM-UHFFFAOYSA-N pyrene-1-carbaldehyde Chemical compound C1=C2C(C=O)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 RCYFOPUXRMOLQM-UHFFFAOYSA-N 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000004304 visual acuity Effects 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0528—Macromolecular bonding materials
- G03G5/0589—Macromolecular compounds characterised by specific side-chain substituents or end groups
Definitions
- This invention relates to an electrophotographic lithographic printing plate precursor, and, more particularly, to a lithographic printing plate precursor having a photoconductive layer on which a surface layer having specific properties is provided.
- a number of offset printing plate precursors for directly producing printing plates have hitherto been proposed, and some of them have already been put into practical use. Widely employed among them is a system in which a photoreceptor comprising a conductive support having provided thereon a photoconductive layer mainly comprising photoconductive particles, e.g., zinc oxide, and a resin binder is subjected to ordinary electrophotographic processing to form a highly lipophilic toner image thereon, and the surface of the photoreceptor is then treated with an oildesensitizing solution called an etching solution to selectively render non-image areas hydrophilic to obtain an offset printing plate.
- an oildesensitizing solution called an etching solution to selectively render non-image areas hydrophilic to obtain an offset printing plate.
- Requirements of offset printing plate precursors for obtaining satisfactory prints are such that: an original should be reproduced faithfully on the photoreceptor; that the surface of a photoreceptor has affinity with an oildesensitizing solution so as to render non-image areas sufficiently hydrophilic and, at the same time, has water resistance; and that a photoconductive layer having formed thereon an image is not attenuated during printing and is sufficiently receptive to dampening water so that the non-image areas retain the hydrophilic properties enough to exhibit freedom from stains even on printing a large number of prints.
- a photoconductive layer comprising particles of an organic photoconductive compound and a binder resin can be formed on a grained aluminum base.
- Printing plate precursors of this type can be produced by forming a toner image on a photosensitive layer through the known electrophotographic processing as described above and removing the non-image areas by eluting with a processing solution, whereby the aluminum base corresponding to the non-image areas is exposed to form hydrophilic areas.
- the photosensitive layer using the organic photoconductive compound comprises, for example, an oxadiazole compound or oxazole compound and an alkali-soluble binder resin, e.g., a styrene-maleic anhydride copolymer, etc., as disclosed in Japanese Patent Publication Nos.
- the surface layer becomes water-soluble upon ring-opening, the surface layer is seriously inferior in water resistance even when the surface layer is composed of the vinyl ether-maleic anhydride copolymer in combination with other compatible hydrophilic resins. Therefore, printing durability of the resulting printing plate is only about 500 to 600 prints at most.
- a surface layer capable of being rendered hydrophilic which comprises silylated polyvinyl alcohol as a main component and a crosslinking agent as disclosed in Japanese Patent Application (OPI) Nos. 90343/85, 159756/85, and 217292/86.
- OPI Japanese Patent Application
- the surface layer on the non-image area can be rendered hydrophilic by hydrolysis of the silylated polyvinyl alcohol.
- the degree of silylation of polyvinyl alcohol is so controlled, and the remaining hydroxyl groups are crosslinked by the crosslinking agent.
- the residual hydroxyl groups cannot be completely crosslinked even by using a crosslinking agent, and the surface layer is rendered conductive by the remaining hydroxyl groups and, therefore, becomes liable to cause charge leakage.
- the surface layer can hardly hold insulation quality equal to that of a photosensitive layer, thus making it difficult to avoid adverse influences on the surface layer, such as reduction in exposure sensitivity.
- the chemical structure of the hydrophilic polymer has limitations which make it difficult to improve charging properties and quality of a reproduced image (e.g., dot reproducibility and resolving power of image areas, resistance to background fog of non-image areas, etc.) without adversely influencing other qualities of an electrophotographic photoreceptor.
- the above method entails cost since achievement of sufficient hydrophilic properties after hydrolysis requires a relatively large quantity of silylated polyvinyl alcohol. Besides, considering the whole balance of performance, such as electrophotographic characteristics, film-forming properties, etc., there is only a narrow choice of material composition.
- One object of this invention is to provide a lithographic printing plate precursor which reproduces an image faithful to an original, forms neither background stains evenly over the entire surface nor dot-like stains, and exhibits excellent oil-desensitivity.
- Another object of this invention is to provide a lithographic printing plate which retains sufficient hydrophilic properties on its non-image areas so as to exhibit stain resistance and high printing durability even when used for printing a large number of prints.
- a further object of this invention is to provide a lithographic printing plate precursor having a surface layer to be rendered hydrophilic on non-image areas, the surface layer comprising a resin which can be synthesized easily.
- a still further object of this invention is to provide a lithographic printing plate precursor which can be produced at a relatively low cost and allowed a wide choice in material composition to aquire a broad range of electrophotographic characteristics, film-forming properties, and the like.
- a lithographic printing plate precursor comprising an electrophotographic photoreceptor which comprises a conductive support having provided thereon at least one photoconductive layer and an outermost surface layer, used for producing an image on the photoconductive layer and then subjecting the layer to an oil-desensitization treatment, in which said surface contains, as a main component, at least one resin selected from the group consisting of (A) a resin obtained by polymerizing at least one monomer having at least one functional group which is capable of forming a hydroxyl group upon decomposition by the oil-desensitization treatment and which is represented by formula:
- L 1 represents ##STR1## wherein R 1 , R 2 , and R 3 , which may be the same or different, each represents a hydrogen atom, a hydrocarbon group or --O--R', wherein R' represents a hydrocarbon group; Y 1 and Y 2 each represents a hydrocarbon group; Z represents an oxygen atom, a sulfur atom or --NH--; and X represents a sulfur atom or an oxygen atom, in the side chain thereof, and (B) a resin obtained by polymerizing at least one monomer having at least one functional group in which at least two hydroxyl groups sterically near to each other are simultaneously protected with one protective group, and which is capable of forming at least two hydroxyl groups upon decomposition by the oil-desensitization treatment.
- the resin (A) comprising at least one monomer unit containing at least one functional group of formula (--O--L) in the side chain thereof can be obtained by polymerizing one or more of such monomers or copolymerizing one or more of such monomers with other copolymerizable monomers.
- the resin (B) containing at least one functional group in which two or more hydroxyl groups sterically near to each other are protected with one protective group can be obtained by a process comprising polymerizing a monomer containing at least two hydroxyl groups which have previously been protected with one protective group or copolymerizing such a monomer with other copolymerizable monomers.
- the functional group where at least one hydroxy group is protected as represented by formula (I), and the functional group where at least two hydroxyl groups are protected with one protective group as represented by formulae (II) to (V) can be formed by the method as described in literature references cited in, for example, New Experimental Chemical Lecture, Vol. 14, Organic Compound Synthesis and Reaction (V), p. 2505 compiled by Japan Chemical Association (published by Maruzen Publishing Co., Ltd.); T.W. Green, "Protective Groups in Organic Synthesis", Chapters 2 and 3 (John and Willey, 1981); J.F.W. Mc.Omie, "Protective Groups in Organic Chemistry", Chapters 3 and 4 (Prenum. Press), etc.
- the functional group of formula (--O--L) in the resin (A) is capable of forming a hydroxyl group upon being decomposed.
- R 3 each preferably represents a hydrogen atom, a substituted or unsubstituted straight or branched chain alkyl group having from 1 to 18 carbon atoms (e.g., methyl, ethyl, propyl, butyl, hexyl, octyl, decyl, dodecyl, octadecyl, chloromethyl, dichloroethyl, methoxyethyl, and methoxypropyl groups), a substituted or unsubstituted alicyclic group (e.g., cyclopentyl, and cyclohexyl groups), a substituted or unsubstituted aralkyl group having from 7 to 12 carbon atoms (e.g., benzyl, phenethyl, chlorobenzyl, and methoxybenzyl groups),
- Y 1 preferably represents a substituted or unsubstituted straight chain or branched chain alkyl group having from 1 to 6 carbon atoms (e.g., methyl, trichloromethyl, trifluoromethyl, methoxymethyl, phenoxymethyl, 2,2,2-trifluoroethyl, t-butyl, and hexafluoroisopropyl groups), a substituted or unsubstituted aralkyl group having from 7 to 9 carbon atoms (e.g., benzyl, phenethyl, methylbenzyl, trimethylbenzyl, heptamethylbenzyl, and methoxybenzyl groups), or a substituted or unsubstituted aryl group having from 6 to 12 carbon atoms (e.g., phenyl, nitrophenyl cyanophenyl, methanesulfonylphenyl, methoxyphenyl,
- Y represents an oxygen atom, a sulfur atom or an --NH-- bond; and Y 2 has the same meaning as Y 1 .
- the monomer having at least one functional group of formula (--O--L) in the side chain thereof includes, for example, compounds of formula (I): ##STR4## wherein X, represents --O--, --CO--, --COO--, --OCO--, ##STR5## an aromatic group or a heterocyclic ring, wherein Q 1 , Q 2 , Q 3 , and Q 4 each represents a hydrogen atom, a hydrocarbon group or the group (Y'--O--L) in formula (I); b 1 and b 2 , which may be the same or different, each represents a hydrogen atom, a hydrocarbon group or the group (Y'--O--L) in formula (I); and n represents 0 or an integer of from 1 to 18; Y' represents a carbon-carbon bond connecting X' with --O--L which may contain a hetero atom (examples of a hetero atom including an oxygen atom, a sulfur atom, and a nitrogen atom
- b 3 , b 4 , and b 5 each has the same meaning as b 1 and b 2 ); and a 1 and a 2 , which may be the same or different, each represents a hydrogen atom, a hydrocarbon group (e.g., an alkyl group having from 1 to 12 carbon atoms which may be substituted with --COOH, etc.), --COOH or --COOW, wherein W represents an alkyl group having from 1 to 18 carbon atoms, an alkenyl group, an aralkyl group, an alicyclic group or an aromatic group, each of which may be substituted with a group selected from groups including (--O--L).
- a hydrocarbon group e.g., an alkyl group having from 1 to 12 carbon atoms which may be substituted with --COOH, etc.
- W represents an alkyl group having from 1 to 18 carbon atoms, an alkenyl group, an aralkyl group, an alicyclic group or an aromatic group, each
- These monomers can be prepared by 1) converting a hydroxyl group(s) of a compound having a polymerizable double bond and at least one hydroxyl group to the functional group of formula (--O--L) according to, for example, the method described in Nihon Kagakukai (ed.), Shinjikken Kagaku Koza, Vol. 14, "Yuki Kagobutsu no Gosei to Han-no (V)", p. 2497, Maruzen K.K. or 2) reacting a compound having the functional group of formula (--O--L) with a compound having a polymerizable double bond.
- R 4 and R 5 which may be the same or different, each represents a hydrogen atom, a hydrocarbon group or --O--R", wherein R" represents a hydrocarbon group; and W represents a carbon-carbon bond or bonding group which may contain a hetero atom, the number of atoms between the oxygen atoms being limited to 5 or less; ##STR9## wherein W is as defined above; ##STR10## wherein R 4 , R 5 , and W are as defined above; and ##STR11## wherein R 4 and R 5 are as defined above, and R 6 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, for example, a methyl, ethyl, propyl or butyl group.
- R 4 and R 5 each preferably represents a hydrogen atom, a substituted or unsubstituted alkyl group having from 1 to 12 carbon atoms (e.g., methyl, ethyl, propyl, butyl, hexyl, 2-methoxyethyl, and octyl groups), a substituted or unsubstituted aralkyl group having from 7 to 9 carbon atoms (e.g., benzyl, phenethyl, methylbenzyl, methoxybenzyl, and chlorobenzyl groups), an alicyclic group having from 5 to 7 carbon atoms (e.g., cyclopentyl and cyclohexyl groups), a substituted or unsubstituted aryl group (e.g., phenyl, chlorophenyl, methoxyphenyl, methylphenyl, and
- W represents a carbon-carbon bond which may contain a hetero atom, with the number of atoms between two oxygen atoms being limited to 5 or less.
- the resin which can be used in the present invention can be prepared by polymerizing at least one monomer containing the functional group or copolymerizing such a monomer with other copolymerizable monomers.
- the above-described method comprising polymerization of a monomer previously containing the functional group in the side chain thereof is preferable to a method comprising converting a hydroxyl group in a polymer to a hydrophobic group because the functional group in the polymer can be controlled arbitrarily in kind and amount and also incorporated of by-products or impurities accompanying high-molecular reaction, etc. into the polymer can be avoided thereby to improve stability of performance properties, such as electrophotographic characteristics.
- the above-described monomers may be copolymerized with other copolymerizable monomers having various performance properties.
- polymer resins having a desired chemical structure can be obtained by incorporating a comonomer unit having satisfactory film-forming properties
- V represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms (e.g., a methyl, ethyl, propyl or butyl group); and/or a reactive comonomer unit which enhances film strength through self-crosslinking, such as ##STR14## wherein V' represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and the like.
- a polymer having a sufficient film strength can also be obtained, without using any crosslinking agent, by, for example, adjusting an average molecular weight of the resulting polymer to about 100,000 or more and/or appropriately selecting a type of the comonomer used.
- copolymerizable monomers include vinyl or allyl esters of aliphatic carboxylic acids, e.g., vinyl acetate, vinyl propionate, vinyl butyrate, allyl acetate, allyl propionate, etc.; unsaturated carboxylic acids, e.g., acrylic acid, methacrylic acid, crotonic acid, itaconic acid, maleic acid, fumaric acid, etc., and esters or amides thereof; styrene derivatives, e.g., styrene, vinyltoluene, ⁇ -methylstyrene, etc.; ⁇ -olefins; acrylonitrile, methacrylonitrile; vinyl-substituted heterocyclic compounds, e.g., N-vinylpyrrolidone, etc.; and the like.
- unsaturated carboxylic acids e.g., acrylic acid, methacrylic acid, crotonic acid, itaconic
- a crosslinking reaction can be taken advantage of as hereinafter described.
- a monomer containing a functional group which can easily undergo crosslinking such as epoxy, amino, isocyanate, carboxyl and hydroxyl groups. Details for such copolymerization are described in references cited in Nihon Kgakukai (ed.), Shinjikken Kagaku Koza, Vol. 14, "Yuki Kagobutsu no Gosei to Han-no (V)", 2535, Maruzen K.K., and Yoshio Iwakura and Keisuke Kurita, Han-nosei Kobunshi, 170, Kodansha.
- the resin A) or B) comprising the functional group-containing monomer component according to the present invention is a homo- or copolymer comprising from 40 to 100% by weight of a monomer component containing the functional group, and preferably a copolymer comprising from 40 to 80% by weight of such a monomer component.
- the resin according to the present invention has a molecular weight of from 1 ⁇ 10 3 to 1 ⁇ 10 6 , and preferably from 5 ⁇ 10 3 to 5 ⁇ 10 5 .
- conventionally known resins may also be used in combination with the above-described resins according to the present invention.
- resins include silicone resins, alkyd resins, vinyl acetate resins, polyester resins, styrene-butadiene resins, acrylic resins, and the like. Specific examples of these known resins are described, e.g., in T. Kurita et al., Kobunshi, Vol. 17, 278 (1968), H. Miyamoto et al., Imaging, Vol. 1973, No. 8, 9, etc.
- the mixing ratio of the resin according to the present invention and the known resin is arbitrary as far as the proportion of a component containing the functional group falls within a range of from 40 to 100% by weight, and preferably from 45 to 100% by weight, based on the total resin. If the proportion of the functional group-containing component is less than 40% by weight, the resulting lithographic printing plate precursor does not show sufficient oil-desensitivity when processed with an oil-desensitizing solution or dampening water, thus resulting in stain formation during printing.
- the resin (A) or (B) according to the present invention which contains at least one functional group is capable of forming at least one hydroxyl group when hydrolyzed or hydrogenolyzed upon contact with an oil-desensitizing solution or dampening water used on printing. Therefore, when the resin is used as an outermost surface layer of a lithographic printing plate precursor, non-image areas can be rendered hydrophilic by the action of the hydroxyl group formed in the resin. As a result, a marked contrast can be afforded between lipophilic toner image areas and hydrophilic non-image areas, and adhesion of a printing ink onto the non-image areas during printing can be avoided.
- the resin (B) containing at least one functional group with the two or more hydroxyl groups thereof sterically near to each other being protected with one protective group is capable of forming at least two hydroxyl groups when hydrolyzed or hydrogenolyzed upon contact with an oil-desensitizing solution or dampening water used on printing.
- an oil-desensitizing solution or dampening water used on printing As a result, sufficiently high hydrophilic properties can be attained to effectively produce the effects of the surface layer in spite of a small content of the functional group. Therefore, the resin can be produced at a relatively low cost.
- selection may be made from a wide choice of material composition in adjusting the whole balance of performance properties, such as electrophotographic characteristics, film-forming properties, etc.
- the surface layer of the present invention may further contain resins other than those described above, as well as crosslinking agents, plasticizers, and the like.
- the crosslinking agent to be added includes generally employed organic peroxides, metallic soaps, organic silane compounds, polyurethane, and curing agents, e.g., epoxy resins. Specific examples of these crosslinking agents are described, e.g., in S. Yamashita and T. Kaneko (Eds.), Kakyozai Handbook, Taiseisha (1981).
- the matting agent to be added includes fillers, e.g., silicon dioxide, zinc oxide, titanium oxide, zirconium oxide, glass beads, alumina, clay, etc., and polymer particles, e.g., polymethyl methacrylate, polystyrene, phenolic resins, etc.
- the non-image areas thereof should become sufficiently hydrophilic after oil-desensitization as mentioned before.
- the hydrophilic properties of the non-image areas can be confirmed, for example, by measuring a contact angle formed with water. While the contact angle with water of the surface layer before oil-desensitization is from about 60° to 120° , it is decreased to about 50 to 20° C. after oil-desensitization to attain high wettability by water. Hence, the resulting printing plate has formed thereon lipophilic toner image areas and highly hydrophilic non-image areas. It is preferable that the contact angle with water be decreased to 20° or less by oil-desensitization processing.
- the lithographic printing plate precursor according to the present invention is particularly superior in hydrophilic properties on non-image areas as compared with conventional ones.
- the electrophotographic photosensitive layer i.e., photoconductive layer, to be used in the present invention can be formed by using any conventional photoconductive substances, either organic or inorganic.
- the inorganic photoconductive substances which may be used include zinc oxide, titanium oxide, zinc sulfide, selenium, selenium alloys, cadmium sulfide, cadmium selenide, silicone, etc. These inorganic substances can be used to form a photoconductive layer either alone by deposition in vacuo, sputtering, or the like technique or in combination with a binder resin.
- the organic photoconductive substances which can be used include high-molecular compounds, such as (1) the polyvinylcarbazole or derivatives thereof described in Japanese Patent Publication No. 10966/59, (2) the vinyl polymers described in Japanese Patent Publication Nos. 18674/68 and 19192/68, e.g., polyvinylpyrene, polyvinylanthracene, poly-2-vinyl-4-(4'-dimethylaminophenyl)-5-phenyl-oxazole, poly-3-vinyl-N-ethylcarbazole, etc., (3) the polymers described in Japanese Patent Publication No.
- high-molecular compounds such as (1) the polyvinylcarbazole or derivatives thereof described in Japanese Patent Publication No. 10966/59, (2) the vinyl polymers described in Japanese Patent Publication Nos. 18674/68 and 19192/68, e.g., polyvinylpyrene, polyvinylanthracene, poly-2-vinyl-4-(
- photoconductive substances can be used either individually or in combinations of two or more thereof.
- poly-N-vinylcarbazole preferred are poly-N-vinylcarbazole; triarylamines, e.g., tri-p-tolylamine, triphenylamine, etc.; polyarylmethanes, e.g., 4,4'-bis(diethylamine)-2,2'-dimethyltriphenylmethane, etc.; and unsaturated heterocyclic ring-containing compounds exemplified by pyrazoline derivatives, e.g., 3-(4-dimethylaminophenyl)-1,5-diphenyl-2-pyrazoline, etc.
- pyrazoline derivatives e.g., 3-(4-dimethylaminophenyl)-1,5-diphenyl-2-pyrazoline, etc.
- Binders to be combined with the photoconductive substance are conventional. Typical examples of the known binders are vinyl chloride-vinyl acetate copolymers, styrene-butadiene copolymers, styrene-butyl methacrylate copolymers, polymethacrylate, polyacrylate, polyvinyl acetate, polyvinyl butyral, alkyd resins, silicone resins, epoxy resins, epoxy ester resins, polyester resins, etc.
- the photoconductive substances may also be combined with aqueous acrylic emulsions or acrylic ester emulsions.
- the amount of the binder to be used in the photoconductive layer is generally subject to variation.
- the typical amount of the binder ranges from about 10 to about 90% by weight.
- the resin of the invention may contain known spectral sensitizers, such as xanthene dyes, triphenylmethane dyes, azine dyes, metallized phthalocyanine dyes, polymethine dyes, etc.
- spectral sensitizers such as xanthene dyes, triphenylmethane dyes, azine dyes, metallized phthalocyanine dyes, polymethine dyes, etc.
- the photoconductive layer may be composed of a single layer or two or more layers.
- the layer structure includes a so-called separate function type photoconductive layer composed of a charge generating layer comprising a deposit of the above-described photoconductive substance or an organic pigment, e.g., a phthalocyanine dye and an azo dye, and, if desired, a binder resin and a charge transport layer comprising the above-recited high polymeric compound or low polymeric compound and a binder resin.
- the photoconductive layer according to the present invention can be provided on any known support.
- a support for an electrophotographic light-sensitive layer is preferably electrically conductive.
- Any of conventionally employed conductive supports may be utilized in this invention.
- Examples of usable conductive supports include a base (e.g., a metal sheet, paper, a plastic sheet, etc.) having been rendered electrically conductive by, for example, impregnating with a low resistant substance; a base with the back side thereof (opposite to the photosensitive layer side) being rendered conductive and further coated thereon at least one layer for the purpose of prevention of curling, etc.; the aforesaid bases having provided thereon a water-resistant adhesive layer; the aforesaid bases having provided thereon at least one precoat layer; paper laminated with a plastic film on which aluminum, etc. is deposited; and the like.
- the thickness of the photoconductive layer on the support can be selected from a broad range and usually ranges from about 10 to about 300 ⁇ m, and preferably from about 50 to about 150 ⁇ m, on a wet basis. Thickness outside of this range also gives satisfactory results.
- a suitable dry thickness of the photoconductive layer ranges from about 1 to about 50 ⁇ m.
- the surface layer to be rendered hydrophilic has a thickness of 10 ⁇ m or less, and preferably between 0.1 and 5 ⁇ m for particular use for Carson processing. A surface layer thickness exceeding 5 ⁇ m would result in reduction of sensitivity of the photoreceptor and increase of residual potential.
- an electrophotographic photosensitive layer (photoconductive layer) is formed on a conductive support in a usual manner. Then, a solution or dispersion of the resin according to the present invention and, if necessary, additives in a volatile hydrocarbon solvent having a boiling point of 200° C. or lower are coated on the photoconductive layer, followed by drying.
- the organic solvent to be used preferably includes halogenated hydrocarbons having from 1 to 3 carbon atoms, e.g., dichloroethane, chloroform, 1,2-dichloroethane, tetrachloroethane, dichloropropane, and trichloroethane. It is also possible to use other various solvents commonly employed for coating, such as aromatic hydrocarbons (e.g., chlorobenzene, toluene, xylene, benzene, etc.), ketones (e.g., acetone, 2-butanone, etc.), ethers (e.g., tetrahydrofuran, etc.), methylene chloride, and so on, and mixtures thereof.
- aromatic hydrocarbons e.g., chlorobenzene, toluene, xylene, benzene, etc.
- ketones e.g., acetone, 2-butanone, etc.
- ethers e.
- a toner image is then formed on the thus obtained printing plate precursor in accordance with ordinary electrophotographic processing, and the surface is treated with an oil-desensitizing solution, for example, an acidic or alkaline aqueous solution, and an aqueous solution of a reducing agent, thereby to render the non-image area hydrophilic.
- an oil-desensitizing solution for example, an acidic or alkaline aqueous solution, and an aqueous solution of a reducing agent, thereby to render the non-image area hydrophilic.
- formation of a toner image can be effected, for example, by (1) a method comprising forming an electrostatic latent image on a separate electrophotographic photoreceptor, electrostatically transferring the latent image to the printing plate precursor of the invention, and developing the transferred image to form a toner image, (2) a method comprising applying electrical signals to a multi-needle electrode to form an electrostatic latent image corresponding to the electrical signals on the photoreceptor and developing the latent image to obtain a toner image, or (3) a method comprising forming an electrostatic latent image on an electrophotographic photoreceptor in the form of a screen having a number of fine openings, subjecting the photoreceptor to corona discharge through the latent image to modulate the ionic stream of corona to form an electrostatic latent image, and developing the latent image with a toner.
- the present invention can be applied to any of these toner image formation systems.
- a lithographic printing plate precursor comprising forming an electrostatic latent image
- the surface layer of the present invention which can be rendered hydrophilic makes it possible to utilize any of the known electrophotographic photoreceptors to form a high quality lithographic printing plate precursor.
- the surface layer achieves both highly hydrophilic properties and water resistance after oil-desensitization. Further, the surface layer exhibits very satisfactory adhesion to both the base and a toner image so that the resulting printing plate precursor has markedly improved resistance to background staining as well as high printing durability.
- the lithographic printing plate precursor of the present invention substantially retains the sensitivity inherent to an electrophotographic photosensitive layer after storage, it has a much higher sensitivity as compared with conventional ones.
- the lithographic printing plate precursor of the present invention may have its functions separated into a photoconductive layer and a surface layer to be rendered hydrophilic thereby broadening the range of choice of material. For instance, selection of a material having high sensitivity in the longer wavelength region would realize a recording system using an He-Ne laser or a semi-conductor laser, which has hitherto been impossible.
- oil-desensitization of the printing plate precursor of the present invention to render non-image areas hydrophilic can be carried out simply by dipping the precursor in an oil-desensitizing solution for several seconds, thus making it possible to produce a printing plate by means of a small-sized and simple apparatus.
- the resulting photosensitive was coated on a transparent conductive support composed of a 100 ⁇ m thickn polyethylene terephthalate film having a deposit film of indium oxide (surface resistivity: 10 3 ⁇ ) by means of a wire round rod to form an organic photosensitive layer having a thickness of about 4 ⁇ m.
- a mixed solution consisting of 50 g of n-butyl methacrylate, 50 g of Compound (2) according to the present invention, and 400 g of toluene was heated to 75° C. in a nitrogen stream.
- To the mixture was added 1.5 g of azobisisobutyronitrile (AIBN), and the mixture was allowed to react for 9 hours.
- the resulting copolymer had a weight average molecular weight of 35,000.
- a 5% toluene solution of the copolymer was coated on the above-prepared photoreceptor with a doctor blade to produce an electrophotographic lithographic printing plate precursor having a surface layer of about 2 ⁇ m in thickness.
- the resulting printing plate precursor was passed once through an etching processor using an oil-desensitizing solution ("ELP-EX" produced by Fuji Photo Film Co., Ltd.) for oil-desensitization.
- ELP-EX oil-desensitizing solution
- the contact angle formed with water was found to be 16° as measured by a goniometer.
- this result obviously demonstrates that the surface layer of the printing plate precursor was satisfactorily rendered hydrophilic.
- the printing plate precursor was processed in an automatic plate making machine ("ELP 404V” manufactured by Fuji Photo Film Co., Ltd.) by using a negatively chargeable liquid developer to form a toner image and then subjected to oil-desensitization under the same conditions as described above.
- ELP 404V automatic plate making machine
- the resulting printing plate was mounted as offset master on an offset printing machine ("Hamada Star 800SX”manufactured by Hamada Star K.K.), and printing was carried out on fine paper.
- a 5% toluene solution of the copolymer was coated with a doctor blade on the photosensitive layer to form a surface layer of about 2 ⁇ m in thickness.
- the resulting lithographic printing plate precursor was charged to -6 kV by means of a paper analyzer ("SP-428" manufactured by Kawaguchi Denshi K.K.), and the initial potential (V 0 ), dark charge retention (DRR), and half decay exposure (E 1/2 ) were measured.
- the printing plate precursor was processed in an automatic plate making machine "ELP 404V” using a toner "ELP-T".
- the resulting master plate for offset printing had a density of 1.0 or more and a clear image.
- the master plate was mounted on a printing machine to effect printing.
- the print after obtaining 10,000 prints had a clear image without any fog on the non-image area.
- a mixed solution consisting of 27 g of ethyl methacrylate, 70 g of Compound (26) of the present invention, 3 g of 2-hydroxyethyl methacrylate, and 200 g of toluene was subjected to polymerization reaction under the same conditions as in Example 2.
- the resulting copolymer had a weight average molecular weight of 38,000.
- the printing plate precursor was processed in ELP-404V in the same manner as in Example 2.
- the resulting master print for offset printing had a density of 1.0 or more and a clear image. After etching processing, the master plate was used for printing. The print after obtaining 10,000 prints had a clear image free from fog on the non-image area.
- copolymers (D), (E), and (F) having structures in the weight percentages shown in Table 1 below were prepared.
- a lithographic printing plate precursor was produced in the same manner as in Example 1, except for replacing the resin used in the surface layer in Example 1 with each of resins (D) to (F).
- Example 2 The resulting precursors were evaluated for electrostatic characteristics in the same manner as in Example 2. Each of the precursors were then processed in an automatic plate making machine "ELP-404V", and printing was carried out in the same manner as in Example 1 to determine printing durability. The results obtained are shown in Table 2. As is apparent from Table 2, these results are similar to those of Examples 1 and 2.
- a lithographic printing plate precursor was produced in the same manner as in Example 1, except for replacing the resin used in the surface layer of Example 1 with the above-prepared resin.
- a contact angle formed by the resulting printing plate precursor and distilled water before and after oil-desensitization was measured in the same manner as in Example 1 and was found to be 85° and 18° , respectively, indicating that the surface layer of the precursor was satisfactorily rendered hydrophilic by the oil-desensitization processing.
- Example 2 In the same manner as in Example 2, a double-layered photosensitive layer was formed on the same transparent conductive support as used in Example 1 to obtain an electrophotographic photoreceptor.
- a mixed solution consisting of 20 g of benzyl methacrylate, 30 g of ethyl methacrylate, 50 g of Copolymer Component (51) of the present invention, and 300 g of toluene was heated to 75° C. in a nitrogen stream. After adding 1.0 g of AIBN thereto, the mixture was allowed to react for 8 hours. The resulting copolymer had a weight average molecular weight of 45,000.
- a 5% toluene solution of the copolymer was coated with a doctor blade on the double-layered photosensitive layer to form a surface layer having a thickness of about 2 ⁇ m.
- a master plate for offset printing obtained from the printing plate precursor in the same manner as in Example 1 had a density of 1.0 or more and a clear image. After etching processing, printing test was carried out. The print after obtaining 10,000 prints had a clear image free from fog on the non-image area.
- a mixed solution consisting of 37 g of n-butyl methacrylate, 60 g of Compound (51) of the present invention, 3 g of 2-hydroxyethyl methacrylate, and 200 g of toluene was subjected to polymerization reaction under the same conditions as in Example 8.
- the resulting copolymer had a weight average molecular weight of 38,000.
- a master plate for offset printing obtained from the printing plate precursor in the same manner as in Example 1 had a density of 1.0 or more and a clear image. After etching processing, a printing test was carried out. The print after obtaining 10,000 prints had a clear image free from fog on the non-image area.
- a mixed solution consisting of 40 g of butyl vinyl ether, 10 g of 4-methylene-1,3-dioxoran, and 100 g of ethyl ether was cooled to -78° C. in a nitrogen stream, and 5 g of a boron trifluoride ethyl etherate was added thereto while stirring, followed by reacting for 60 hours.
- a methanolic solution of ammonia was added to the reaction system to step the polymerization. The precipitated polymer was separated from the solvent by decantation, washed with n-hexane, and dried under reduced pressure.
- a 5% toluene solution containing the above prepared copolymer and a butyl methacrylate/acrylic acid (98/2 by weight) copolymer at a weight ratio of 8/2 was coated on the same photoreceptor as prepared in Example 8 with a doctor blade and dried at 110° C. for 1 minute to form a surface layer having a thickness of about 1.8 ⁇ m.
- a master plate for offset printing obtained from the printing plate precursor in the same manner as in Example 1 had a density of 1.0 or more and a clear image. After etching processing, a printing test was carried out. The print after obtaining 10,000 prints had a clear image free from fog on the non-image area.
- a lithographic printing plate precursor was produced in the same manner as in Example 7, except for replacing the resin used in the surface layer of Example 7 with each of the resins (G), (H), and (I) shown in Table 3.
- Example 2 The electrostatic characteristics of the resulting precursor were determined in the same manner as in Example 2. An offset master plate obtained from the precursor in the same manner as in Example 1 was subjected to a printing test. The results obtained are shown in Table 4.
- the surface layer comprising the specific resin according to the present invention achieves both high hydrophilic properties and water resistance upon oil-desensitization and also exhibits excellent adhesion to a base as well as retentiveness of toner image.
- the electrophotographic lithographic printing plate precursor having such a surface layer possesses superior quality in both background stain resistance and printing durability.
- the resins to be used in the present invention can be prepared easily.
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- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Printing Plates And Materials Therefor (AREA)
Abstract
--O--L
Description
--O--L
V.sub.0 =-540 V
DRR=84%
E.sub.1/2 =54.5 erg/cm.sup.2.
TABLE 1 __________________________________________________________________________ Resin Structure __________________________________________________________________________ (D) ##STR19## (E) ##STR20## (F) ##STR21## __________________________________________________________________________
TABLE 2 ______________________________________ Example 4 Example 5 Example 6 Resin (D) (E) (F) ______________________________________ Electrostatic Characteristics: V.sub.0 (V) 570 580 565 DRR (%) 84 86 83 E.sub.1/2 (erg/cm.sup.2) 57.3 56.2 56.0 Image Quality After Plate Making: Density 1.0 1.0 1.0 or more or more or more Image Quality clear clear clear Printing Durability 10,000 10,000 10,000 or more or more or more ______________________________________
V.sub.0 =-580 V
DRR=87%, and
E.sub.1/2 =56 erg/cm.sup.2.
V.sub.0=- 540 V
DRR=84%, and
E.sub.1/2 =54.5 erg/cm.sup.2.
TABLE 3 ______________________________________ Example No. Resin Monomers Weight Ratio ______________________________________ 11 (G) n-butyl methacrylate 50 monomer corresponding to 50 Component (42) 12 (H) n-butyl methacrylate 40 monomer corresponding to 60 Component (42) 13 (I) ethyl methacrylate 50 monomer corresponding to 50 Component (52) ______________________________________
TABLE 4 ______________________________________ Example 11 Example 12 Example 13 Resin (G) (H) (I) ______________________________________ Electrostatic Characteristics: V.sub.0 (V) 580 570 560 DRR (%) 85 85 86 E.sub.1/2 (erg/cm.sup.2) 56.5 55.2 54.3 Image Quality After Plate Making: Density 1.0 1.0 1.0 or more or more or more Image Quality clear clear clear Printing Durability 10,000 10,000 10,000 or more or more or more ______________________________________
Claims (11)
--O--L
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10641787A JPS63272551A (en) | 1987-05-01 | 1987-05-01 | Original plate for lithographic press |
JP62-106417 | 1987-05-01 | ||
JP62-151507 | 1987-06-19 | ||
JP15150787A JPH01272489A (en) | 1987-06-19 | 1987-06-19 | Original plate for lithographic printing |
Publications (1)
Publication Number | Publication Date |
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US4897328A true US4897328A (en) | 1990-01-30 |
Family
ID=26446525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/188,824 Expired - Lifetime US4897328A (en) | 1987-05-01 | 1988-05-02 | Electrophotographic lithographic printing plate precursor |
Country Status (2)
Country | Link |
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US (1) | US4897328A (en) |
EP (1) | EP0289056A3 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5219705A (en) * | 1988-07-04 | 1993-06-15 | Fuji Photo Film Co., Ltd. | Lithographic printing plate precursor of direct image type |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3930584A1 (en) * | 1989-09-13 | 1991-03-14 | Basf Ag | OFFSET PRINTING PLATE PRODUCED ON ELECTROPHOTOGRAPHIC WAY WITH HYDROPHILIC CONCRETE AREAS AND OLEOPHILIC UNCOVERAGE AREAS |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4673627A (en) * | 1984-12-27 | 1987-06-16 | Fuji Photo Film Co., Ltd. | Electrophotographic lithographic printing plate |
US4724195A (en) * | 1984-06-08 | 1988-02-09 | Hoechst Aktiengesellschaft | Perfluoroalkyl group-containing copolymers and reproduction layers produced therefrom |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS60205455A (en) * | 1984-03-30 | 1985-10-17 | Toyo Ink Mfg Co Ltd | Electrophotographic sensitive body |
-
1988
- 1988-04-29 EP EP88106950A patent/EP0289056A3/en not_active Ceased
- 1988-05-02 US US07/188,824 patent/US4897328A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4724195A (en) * | 1984-06-08 | 1988-02-09 | Hoechst Aktiengesellschaft | Perfluoroalkyl group-containing copolymers and reproduction layers produced therefrom |
US4673627A (en) * | 1984-12-27 | 1987-06-16 | Fuji Photo Film Co., Ltd. | Electrophotographic lithographic printing plate |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5219705A (en) * | 1988-07-04 | 1993-06-15 | Fuji Photo Film Co., Ltd. | Lithographic printing plate precursor of direct image type |
Also Published As
Publication number | Publication date |
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EP0289056A2 (en) | 1988-11-02 |
EP0289056A3 (en) | 1990-01-24 |
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